Clinical Research Coordinator

PERKS Full Benefits Package - Medical, Vision, Dental and Life Insurance 401k + Employer Matching Paid Time Off (PTO) and Paid Holidays Paid Maternity Leave Eyecare Certification Reimbursement Competitive Base Pay Employee Discounts

JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily operations of clinical trials. Duties include administration; project implementation, meeting support, quality assurance, and dissemination of results, recruitment; collection, recording, and editing of interview, questionnaire, and clinical data; performing quality assurance monitoring of study data; randomization of study participants; conducting case management tasks; scheduling participant appointments; supporting clinical and group intervention; review medical records following study protocols; and performing other duties in support of clinical trials services as assigned.

Qualifications

Demonstrated interpersonal, communication and interviewing skills with people of all ages. Organized, detail oriented, self-directed and dependable. Able to prioritize work, solve problems and work independently. Able to function in a team environment and use negotiation skills. Favorable result on background check required. Must be able to provide proof of identity and right to work in the United States.

EDUCATION AND/OR EXPERIENCE High school diploma or general education degree (GED) required Undergraduate degree in a related field preferred At least one (1) year of experience collecting information using one of the following methods: Telephone/face-to-face interviews Working with patients and study participants in a clinical situation (proficiency in refracting patients needed) One year of experience collecting or processing data for research or Quality Assurance purposes Working knowledge of medical terminology, anatomy, and disease processes; medical record organization and interpretation Experience in health research or research data collection is preferred Familiarity with classification of disease processes is preferred Knowledge of basic research ethics and principles is preferred

LICENSES AND CREDENTIALS Minimum Required: None

SYSTEMS AND TECHNOLOGY Proficient in Microsoft Excel, Word, PowerPoint, Outlook Basic knowledge of computer functions Able to use computers and software programs for complex tracking of participant tasks

• PHYSICAL REQUIREMENTS This role requires a variety of physical activities to effectively perform essential job functions.
• The position involves frequent walking (75%), sitting (50%), and standing (50%), with regular bending, stooping, and reaching (25–50%).
• Employees must be able to lift, carry, push, and pull items up to 25 lbs.
• Strong fine motor skills and full use of hands are essential, as the role demands constant grasping, writing/typing, and use of technology.
• Visual and auditory acuity—including color, depth, peripheral vision, and the ability to adjust focus—is required 100% of the time.
• Occasional driving or climbing may also be necessary.
• If you need assistance with this application, please contact (636) 227-2600.
• Please do not contact the office directly – only resumes submitted through this website will be considered.
• EyeCare Partners is an equal opportunity/affirmative action employer.
• All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.